393855-75-9

Upstream product

• 40682-54-0 ethyl N-benzylideneglycinate 
• 61299-11-4 ethyl 2-aminohexanoate hydrochloride 
• 616-06-8 2-amino-hexanoic acid 
• 542-69-8 1-iodo-butane 

Downstream Products

• 288161-81-9 di-n-butyl-ethanolamine 
• 1345983-70-1 [2-[(2-amino-2-butylhexanyl)thio]-4-bromo-5-(methyloxy)phenyl](phenyl)methanone 
• 1345983-71-2 8-bromo-3,3-dibutyl-7-(methyloxy)-5-phenyl-2,3-dihydro-1,4-benzothiazepine 
• 1345983-72-3 methyl 3,3-dibutyl-7-(methyloxy)-5-phenyl-2,3-dihydro-1,4-benzothiazepine-8-carboxylate 
• 1345983-73-4 [3,3-dibutyl-7-(methyloxy)-5-phenyl-2,3-dihydro-1,4-benzothiazepin-8-yl]methanol 
• 1345983-74-5 [3,3-dibutyl-7-(methyloxy)-5-phenyl-2,3,4,5-tetrahydro-1,4-benzothiazepin-8-yl]methanol 
• 1345983-75-6 [3,3-dibutyl-7-(methyloxy)-1,1-dioxido-5-phenyl-2,3,4,5-tetrahydro-1,4-benzothiazepin-8-yl]methanol 
• 1345983-76-7 3,3-dibutyl-7-(methyloxy)-5-phenyl-2,3,4,5-tetrahydro-1,4-benzothiazepine-8-carbaldehyde 1,1-dioxide 
• 1345983-77-8 diethyl {[3,3-dibutyl-7-(methyloxy)-1,1-dioxido-5-phenyl-2,3,4,5-tetrahydro-1,4-benzothiazepin-8-yl]methyl}phosphonate 
• 1345983-78-9 8-(bromomethyl)-3,3-dibutyl-7-(methyloxy)-5-phenyl-2,3,4,5-tetrahydro-1,4-benzothiazepine 1,1-dioxide 
• 1345983-26-7 3-({[3,3-dibutyl-7-(methyloxy)-1,1-dioxido-5-phenyl-2,3,4,5-tetrahydro-1,4-benzothiazepin-8-yl]methyl}amino)pentanedioic acid trifluoroacetate 
• 1345984-20-4 dimethyl 3-({[3,3-dibutyl-7-(methyloxy)-1,1-dioxido-5-phenyl-2,3,4,5-tetrahydro-1,4-benzothiazepin-8-yl]methyl}amino)pentanedioate 
• 1345983-28-9 N-{[3,3-dibutyl-7-(methyloxy)-1,1-dioxido-5-phenyl-2,3,4,5-tetrahydro-1,4-benzothiazepin-8-yl]methyl}glycine trifluoroacetate 
• 1345984-21-5 1,1-dimethylethyl N-{[3,3-dibutyl-7-(methyloxy)-1,1-dioxido-5-phenyl-2,3,4,5-tetrahydro-1,4-benzothiazepin-8-yl]methyl}glycinate 

Relevant academic research and scientific papers

CHEMICAL COMPOUNDS

Compounds of Formula (I) and methods for treating metabolic disorders are disclosed.

Synthesis and use of achiral oxazolidine-2-thiones in selective preparation of trans 2,5-disubstituted tetrahydrofurans

The use of achiral N-acetyloxazolidine-2-thiones in the C-glycosylation of lactol acetates has allowed us to prepare with high diastereoselectivity the expected trans 2,5-disubstituted tetrahydrofurans. A study based on the role of the steric hindrance of the N-acetyloxazolidine-2-thiones is reported. Wiley-VCH Verlag GmbH & Co. KGaA, 2009.